rs782490558
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs782490558(-;-) |
Make rs782490558(-;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 133352101 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs782490558 |
dbSNP (classic) | rs782490558 |
ClinGen | rs782490558 |
ebi | rs782490558 |
HLI | rs782490558 |
Exac | rs782490558 |
Gnomad | rs782490558 |
Varsome | rs782490558 |
LitVar | rs782490558 |
Map | rs782490558 |
PheGenI | rs782490558 |
Biobank | rs782490558 |
1000 genomes | rs782490558 |
hgdp | rs782490558 |
ensembl | rs782490558 |
geneview | rs782490558 |
scholar | rs782490558 |
rs782490558 | |
pharmgkb | rs782490558 |
gwascentral | rs782490558 |
openSNP | rs782490558 |
23andMe | rs782490558 |
SNPshot | rs782490558 |
SNPdbe | rs782490558 |
MSV3d | rs782490558 |
GWAS Ctlg | rs782490558 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs782490558(-;-) |
Alt | rs782490558(-;-) |
Reference | Rs782490558(CT;CT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136218956_136218957delCT |
CLNSRC | |
CLNACC | RCV000198901.1, |